Variant #0000046759 (NC_000014.8:g.68292235C>T, NM_133509.3:c.139C>T (RAD51B))

Chromosome 14
Allele Maternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.68292235C>T
DNA change (hg38) g.67825518C>T
Published as -
ISCN -
DB-ID RAD51B_000002
Variant remarks variant marked as interesting (probably affects gene function with phenotypic consequences) but submitter has not yet sufficient evidence to publish - please contact me
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 1
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-07-11 13:49:13 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51B NM_133509.3 +?/? 3 c.139C>T r.(?) p.(Arg47*)


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